Literature DB >> 9436786

Tangential migration of ameboid microglia in the developing quail retina: mechanism of migration and migratory behavior.

J L Marín-Teva1, A Almendros, R Calvente, M A Cuadros, J Navascués.   

Abstract

Long distance migration of microglial precursors within the central nervous system is essential for microglial colonization of the nervous parenchyma. We studied morphological features of ameboid microglial cells migrating tangentially in the developing quail retina to shed light on the mechanism of migration and migratory behavior of microglial precursors. Many microglial precursors remained attached on retinal sheets containing the inner limiting membrane covered by a carpet of Müller cell endfeet. This demonstrates that most ameboid microglial cells migrate tangentially on Müller cell endfeet. Many of these cells showed a central-to-peripheral polarized morphology, with extensive lamellipodia spreading through grooves flanked by Müller cell radial processes, to which they were frequently anchored. Low protuberances from the vitreal face of microglial precursors were firmly attached to the subjacent basal lamina, which was accessible through gaps in the carpet of Müller cell endfeet. These results suggest a mechanism of migration involving polarized extension of lamellipodia at the leading edge of the cell, strong cell-to-substrate attachment, translocation of the cell body forward, and retraction of the rear of the cell. Other ameboid cells were multipolar, with lamellipodial projections radiating in all directions from the cell body, suggesting that microglial precursors explore the surrounding environment to orient their movement. Central-to-peripheral migration of microglial precursors in the retina does not follow a straight path; instead, these cells perform forward, backward, and sideways movements, as suggested by the occurrence of (a) V-shaped bipolar ameboid cells with their vertex pointing toward either the center or the periphery of the retina, and (b) threadlike processes projecting from either the periphery-facing edge or the center-facing edge of ameboid microglial cells.

Entities:  

Mesh:

Year:  1998        PMID: 9436786     DOI: 10.1002/(sici)1098-1136(199801)22:1<31::aid-glia4>3.0.co;2-b

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  13 in total

Review 1.  Müller glia and phagocytosis of cell debris in retinal tissue.

Authors:  Ruth Bejarano-Escobar; Hortensia Sánchez-Calderón; Josué Otero-Arenas; Gervasio Martín-Partido; Javier Francisco-Morcillo
Journal:  J Anat       Date:  2017-07-10       Impact factor: 2.610

Review 2.  Fine-tuning the central nervous system: microglial modelling of cells and synapses.

Authors:  Anna L Xavier; João R L Menezes; Steven A Goldman; Maiken Nedergaard
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-10-19       Impact factor: 6.237

Review 3.  Oxytocin and microglia in the development of social behaviour.

Authors:  Alicia Gonzalez; Elizabeth A D Hammock
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2022-07-11       Impact factor: 6.671

4.  Very brief focal ischemia simulating transient ischemic attacks (TIAs) can injure brain and induce Hsp70 protein.

Authors:  Xinhua Zhan; Charles Kim; Frank R Sharp
Journal:  Brain Res       Date:  2008-08-05       Impact factor: 3.252

5.  Microglia proliferation is controlled by P2X7 receptors in a Pannexin-1-independent manner during early embryonic spinal cord invasion.

Authors:  Chiara Rigato; Nina Swinnen; Roeland Buckinx; Isabelle Couillin; Jean-Marie Mangin; Jean-Michel Rigo; Pascal Legendre; Hervé Le Corronc
Journal:  J Neurosci       Date:  2012-08-22       Impact factor: 6.167

6.  The reactivity, distribution and abundance of Non-astrocytic Inner Retinal Glial (NIRG) cells are regulated by microglia, acute damage, and IGF1.

Authors:  Christopher P Zelinka; Melissa A Scott; Leo Volkov; Andy J Fischer
Journal:  PLoS One       Date:  2012-09-04       Impact factor: 3.240

7.  Plasticity of primary microglia on micropatterned geometries and spontaneous long-distance migration in microfluidic channels.

Authors:  Susanna Amadio; Adele De Ninno; Cinzia Montilli; Luca Businaro; Annamaria Gerardino; Cinzia Volonté
Journal:  BMC Neurosci       Date:  2013-10-13       Impact factor: 3.288

Review 8.  Microglia Contribution to the Regulation of the Retinal and Choroidal Vasculature in Age-Related Macular Degeneration.

Authors:  C Henrique Alves; Rosa Fernandes; Ana Raquel Santiago; António Francisco Ambrósio
Journal:  Cells       Date:  2020-05-14       Impact factor: 6.600

9.  Expression of inducible nitric oxide synthase (iNOS) in microglia of the developing quail retina.

Authors:  Ana Sierra; Julio Navascués; Miguel A Cuadros; Ruth Calvente; David Martín-Oliva; Rosa M Ferrer-Martín; María Martín-Estebané; María-Carmen Carrasco; José L Marín-Teva
Journal:  PLoS One       Date:  2014-08-29       Impact factor: 3.240

10.  Onset of microglial entry into developing quail retina coincides with increased expression of active caspase-3 and is mediated by extracellular ATP and UDP.

Authors:  María Martín-Estebané; Julio Navascués; Ana Sierra-Martín; Sandra M Martín-Guerrero; Miguel A Cuadros; María-Carmen Carrasco; José L Marín-Teva
Journal:  PLoS One       Date:  2017-08-01       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.